Canonical Allele Identifier: CA1360457377
Gene: KLHL40 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.42688206G= , CM000665.2:g.42688206G= GRCh38
NC_000003.11:g.42729698G= , CM000665.1:g.42729698G= GRCh37
NC_000003.10:g.42704702G= NCBI36
NG_033035.1:g.7688G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000287777.5:c.1217G= MANE Select ENSP00000287777.4:p.Gly406=
ENST00000287777.4:c.1217G= ENSP00000287777.4:p.Gly406=
NM_152393.3:c.1217G= NP_689606.2:p.Gly406=
XM_005264866.2:c.1217G= XP_005264923.1:p.Gly406=
NM_152393.4:c.1217G= MANE Select NP_689606.2:p.Gly406=
Search 100 bp 5'
Search 100 bp 3'